Actively Recruiting
Memory Training in Insomnia With Cognitive Impairment
Led by Xuanwu Hospital, Beijing · Updated on 2025-05-28
70
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This randomized controlled trial investigates the effects of Cognitive Remediation Therapy (CRT) on chronic insomnia (CI) with mild cognitive impairment.
CONDITIONS
Official Title
Memory Training in Insomnia With Cognitive Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of Insomnia Disorder according to DSM-5
- Pittsburgh Sleep Quality Index (PSQI) total score greater than 5
- Age 8 years or older
- Voluntary participation with signed informed consent
- Right-handedness
- Age between 55 and 75 years
- Education duration of 12 years or more
- At least junior high school education level
- Meets Petersen's criteria for mild cognitive impairment with subjective memory complaints lasting 3 months or more
- Global Deterioration Scale (GDS) stage 1-2 and Clinical Dementia Rating (CDR) score 0-0.5
- Memory test scores at least 1.5 standard deviations below age- and education-matched norms: MMSE 24 or higher, MoCA less than 26, ADL score above 26
- Memory impairment as the main deficit with preserved function in other cognitive areas
- Normal daily functioning
- No dementia or major physical or psychiatric disorders affecting brain function
You will not qualify if you...
- Severe physical illnesses or major psychiatric disorders, or risk of suicide
- Diagnosed or suspected sleep breathing disorders, restless legs syndrome, circadian rhythm sleep disorders, or shift work
- Pregnancy or breastfeeding
- Currently receiving any psychological therapy
- History of infectious diseases such as syphilis or HIV
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Xuanwu Hospital, Capital Medical University
Beijing, China, 100053
Actively Recruiting
Research Team
H
Hongxing Wang, MD & PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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